在日本EVT引入期间接受EVT或静脉rt-PA治疗的卒中患者手术量与30天死亡率之间的关系

IF 1.9 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Koutarou Matsumoto, Megumi Maeda, Ryu Matsuo, Haruhisa Fukuda, Tetsuro Ago, Takanari Kitazono, Masahiro Kamouchi, Fumi Irie
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引用次数: 0

摘要

本研究旨在确定手术量是否与血管内血栓切除术(EVT)或静脉重组组织纤溶酶原激活剂(IV rt-PA)在日本引入EVT期间治疗卒中后30天死亡率相关。使用全国索赔记录,我们调查了2014年4月至2016年2月期间日本有EVT能力和没有EVT能力的医院中分别接受EVT的8,227名患者和13,406名和6,035名接受rt-PA单药治疗的患者的数据。根据每年在医院进行的evt或静脉注射rt-PA的数量的分位数,将手术量分为三组。分层逻辑回归显示,即使校正了潜在的混杂因素,中等规模医院EVT术后30天死亡率的比值比(95%置信区间)(0.77[0.62-0.96])和高规模医院EVT术后30天死亡率的比值比(0.69[0.53-0.89])也显著低于低规模医院。广义加性混合模型显示EVT对降低死亡风险没有明显的阈值。相比之下,在没有EVT能力的医院,静脉注射rt-PA单药治疗后的死亡风险没有降低,但在有EVT能力的医院,静脉注射rt-PA容量增加会降低死亡风险(异质性P为0.003)。急性缺血性脑卒中EVT术后30天死亡风险随各医院EVT手术量的增加呈线性下降。然而,静脉rt- PA容量与死亡风险之间的关系被医院的EVT能力所修正。需要进一步的研究来确定我们观察到的量-结果关系是EVT后的暂时现象还是随时间的一致趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between procedure volume and 30-day mortality in stroke patients treated with EVT or IV rt-PA during the introduction period of EVT in Japan.

This study aimed to determine whether procedure volume is associated with 30-day mortality following endovascular thrombectomy (EVT) or intravenous recombinant tissue plasminogen activator (IV rt-PA) for stroke during the introduction period of EVT in Japan. Using nationwide claims records, we investigated data from 8,227 patients undergoing EVT and 13,406 and 6,035 patients undergoing rt-PA monotherapy in hospitals with and without EVT capability, respectively, between April 2014 and February 2016 in Japan. Procedure volume was categorized into three groups according to tertiles of the annual number of EVTs or IV rt-PA injections performed in the hospitals. Hierarchical logistic regression demonstrated that the odds ratio (95% confidence interval) of 30-day mortality following EVT was significantly lower in middle- (0.77 [0.62-0.96]) and high- (0.69 [0.53-0.89]) volume hospitals than that in low-volume hospitals even after adjusting for potential confounding factors. The generalized additive mixed models revealed no obvious threshold volume of EVT to reduce the mortality risk. By contrast, mortality risk following IV rt-PA monotherapy did not decrease in hospitals without EVT capability but did with increasing IV rt-PA volume in hospitals with EVT capability (P for heterogeneity 0.003). The risk of 30-day mortality after EVT for acute ischemic stroke decreased linearly according to EVT procedure volume in each hospital. However, the association between IV rt- PA volume and mortality risk was modified by the hospital's EVT capability. Further research is warranted to determine whether the volume-outcome relationship we observed is a temporary phenomenon following EVT or a consistent trend over time.

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